Have questions? Visit https://www.reddit.com/r/SNPedia

rs191009474

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs191009474(A;A)
Make rs191009474(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position38606790
GeneSCN5A
is asnp
is mentioned by
dbSNPrs191009474
ClinGenrs191009474
ebirs191009474
HLIrs191009474
Exacrs191009474
Varsomers191009474
Maprs191009474
PheGenIrs191009474
hapmaprs191009474
1000 genomesrs191009474
hgdprs191009474
ensemblrs191009474
gopubmedrs191009474
geneviewrs191009474
scholarrs191009474
googlers191009474
pharmgkbrs191009474
gwascentralrs191009474
openSNPrs191009474
23andMers191009474
23andMe allrs191009474
SNP Nexus

SNPshotrs191009474
SNPdbers191009474
MSV3drs191009474
GWAS Ctlgrs191009474
Max Magnitude0
ClinVar
Risk rs191009474(A;A) rs191009474(T;T)
Alt rs191009474(A;A) rs191009474(T;T)
Reference Rs191009474(C;C)
Significance Untested
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000003.11:g.38648281C>T
CLNSRC ClinVar
CLNACC RCV000058382.3,